KEGG   Homo sapiens (human): 3181
Entry
3181              CDS       T01001                                 
Symbol
HNRNPA2B1, HNRNPA2, HNRNPB1, HNRPA2, HNRPA2B1, HNRPB1, IBMPFD2, OPMD2, RNPA2, SNRPB1
Name
(RefSeq) heterogeneous nuclear ribonucleoprotein A2/B1
  KO
K13158  heterogeneous nuclear ribonucleoprotein A2/B1
Organism
hsa  Homo sapiens (human)
Pathway
hsa05014  Amyotrophic lateral sclerosis
Network
nt06547  Spliceosome
  Element
N01968  Spliceosome assembly (E and A complex formation)
N01995  mRNA export to the cytoplasm
Disease
H00704  Oculopharyngeal muscular dystrophy
H02031  Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09164 Neurodegenerative disease
   05014 Amyotrophic lateral sclerosis
    3181 (HNRNPA2B1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03019 Messenger RNA biogenesis [BR:hsa03019]
    3181 (HNRNPA2B1)
   03041 Spliceosome [BR:hsa03041]
    3181 (HNRNPA2B1)
  09183 Protein families: signaling and cellular processes
   04147 Exosome [BR:hsa04147]
    3181 (HNRNPA2B1)
Messenger RNA biogenesis [BR:hsa03019]
 Eukaryotic type
  mRNA surveillance and transport factors
   Factors involved in mRNA localization
    Trans-acting binding proteins
     3181 (HNRNPA2B1)
Spliceosome [BR:hsa03041]
 Other splicing related proteins
  Spliceosome associated proteins (SAPs)
   hnRNP proteins
    3181 (HNRNPA2B1)
Exosome [BR:hsa04147]
 Exosomal proteins
  Exosomal proteins of haemopoietic cells  (B-cell, T-cell, DC-cell, reticulocyte, and mast cell)
   3181 (HNRNPA2B1)
  Exosomal proteins of colorectal cancer cells
   3181 (HNRNPA2B1)
SSDB
Motif
Pfam: RRM_1 HnRNPA1_LC RRM_7 RRM_PARP14_3
Other DBs
NCBI-GeneID: 3181
NCBI-ProteinID: NP_112533
OMIM: 600124
HGNC: 5033
Ensembl: ENSG00000122566
UniProt: P22626
Structure
LinkDB
Position
7:complement(26189927..26200746)
AA seq 353 aa
MEKTLETVPLERKKREKEQFRKLFIGGLSFETTEESLRNYYEQWGKLTDCVVMRDPASKR
SRGFGFVTFSSMAEVDAAMAARPHSIDGRVVEPKRAVAREESGKPGAHVTVKKLFVGGIK
EDTEEHHLRDYFEEYGKIDTIEIITDRQSGKKRGFGFVTFDDHDPVDKIVLQKYHTINGH
NAEVRKALSRQEMQEVQSSRSGRGGNFGFGDSRGGGGNFGPGPGSNFRGGSDGYGSGRGF
GDGYNGYGGGPGGGNFGGSPGYGGGRGGYGGGGPGYGNQGGGYGGGYDNYGGGNYGSGNY
NDFGNYNQQPSNYGPMKSGNFGGSRNMGGPYGGGNYGPGGSGGSGGYGGRSRY
NT seq 1062 nt   +upstreamnt  +downstreamnt
atggagaaaactttagaaactgttcctttggagaggaaaaagagagaaaaggaacagttc
cgtaagctctttattggtggcttaagctttgaaaccacagaagaaagtttgaggaactac
tacgaacaatggggaaagcttacagactgtgtggtaatgagggatcctgcaagcaaaaga
tcaagaggatttggttttgtaactttttcatccatggctgaggttgatgctgccatggct
gcaagacctcattcaattgatgggagagtagttgagccaaaacgtgctgtagcaagagag
gaatctggaaaaccaggggctcatgtaactgtgaagaagctgtttgttggcggaattaaa
gaagatactgaggaacatcaccttagagattactttgaggaatatggaaaaattgatacc
attgagataattactgataggcagtctggaaagaaaagaggctttggctttgttactttt
gatgaccatgatcctgtggataaaatcgtattgcagaaataccataccatcaatggtcat
aatgcagaagtaagaaaggctttgtctagacaagaaatgcaggaagttcagagttctagg
agtggaagaggaggcaactttggctttggggattcacgtggtggcggtggaaatttcgga
ccaggaccaggaagtaactttagaggaggatctgatggatatggcagtggacgtggattt
ggggatggctataatgggtatggaggaggacctggaggtggcaattttggaggtagcccc
ggttatggaggaggaagaggaggatatggtggtggaggacctggatatggcaaccagggt
gggggctacggaggtggttatgacaactatggaggaggaaattatggaagtggaaattac
aatgattttggaaattataaccagcaaccttctaactacggtccaatgaagagtggaaac
tttggtggtagcaggaacatggggggaccatatggtggaggaaactatggtccaggaggc
agtggaggaagtgggggttatggtgggaggagccgatactga

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